Canonical Allele Identifier: CA366242175

Gene: ARID1B

Linked Data

• dbSNP Id: rs2128375099
• MyVariant Identifiers: chr6:g.157522310T>C (hg19) ; chr6:g.157201176T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157201176T>C , CM000668.2:g.157201176T>C	GRCh38
NC_000006.11:g.157522310T>C , CM000668.1:g.157522310T>C	GRCh37
NC_000006.10:g.157564002T>C	NCBI36
NG_032093.1:g.428247T>C
NG_032093.2:g.428247T>C
NG_066624.1:g.430151T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4792T>C	ENSP00000055163.8:p.Ser1598Pro
ENST00000414678.8:c.4861T>C	ENSP00000412835.3:p.Ser1621Pro
ENST00000637015.2:c.5080T>C	ENSP00000489729.2:p.Ser1694Pro
ENST00000346085.10:c.4831T>C	ENSP00000344546.5:p.Ser1611Pro
ENST00000350026.10:c.4543T>C	ENSP00000055163.7:p.Ser1515Pro
ENST00000414678.7:c.3109T>C	ENSP00000412835.2:p.Ser1037Pro
ENST00000635849.1:c.2272T>C	ENSP00000490948.1:p.Ser758Pro
ENST00000635957.1:c.1903T>C	ENSP00000490385.1:p.Ser635Pro
ENST00000636227.1:n.3414T>C
ENST00000636254.1:n.871T>C
ENST00000636930.2:c.4951T>C MANE Select	ENSP00000490491.2:p.Ser1651Pro
ENST00000636940.1:n.2948T>C
ENST00000637015.1:c.2319T>C
ENST00000637568.1:c.2233T>C
ENST00000637741.1:n.1617T>C
ENST00000637810.1:c.2293T>C	ENSP00000489636.1:p.Ser765Pro
ENST00000637904.1:c.2452T>C	ENSP00000490550.1:p.Ser818Pro
ENST00000647938.1:c.4582T>C	ENSP00000498155.1:p.Ser1528Pro
ENST00000346085.9:c.4582T>C	ENSP00000344546.4:p.Ser1528Pro
ENST00000350026.9:c.4543T>C	ENSP00000055163.7:p.Ser1515Pro
ENST00000414678.6:c.3109T>C	ENSP00000412835.2:p.Ser1037Pro
NM_017519.2:c.4543T>C	NP_059989.2:p.Ser1515Pro
NM_020732.3:c.4582T>C	NP_065783.3:p.Ser1528Pro
XM_005267069.3:c.4702T>C	XP_005267126.2:p.Ser1568Pro
XM_011535984.1:c.3781T>C	XP_011534286.1:p.Ser1261Pro
XM_011535985.1:c.3601T>C	XP_011534287.1:p.Ser1201Pro
XM_011535986.1:c.3361T>C	XP_011534288.1:p.Ser1121Pro
XM_011535987.1:c.2980T>C	XP_011534289.1:p.Ser994Pro
XM_011535988.1:c.1843T>C	XP_011534290.1:p.Ser615Pro
NM_001346813.1:c.4702T>C	NP_001333742.1:p.Ser1568Pro
NM_001363725.1:c.2452T>C	NP_001350654.1:p.Ser818Pro
XM_011535984.2:c.4912T>C	XP_011534286.2:p.Ser1638Pro
XM_011535988.3:c.1843T>C	XP_011534290.1:p.Ser615Pro
XM_017011103.2:c.4813T>C	XP_016866592.1:p.Ser1605Pro
XM_017011104.1:c.4783T>C	XP_016866593.1:p.Ser1595Pro
XM_017011105.2:c.4753T>C	XP_016866594.1:p.Ser1585Pro
XM_017011106.2:c.4624T>C	XP_016866595.1:p.Ser1542Pro
XM_017011107.2:c.4603T>C	XP_016866596.1:p.Ser1535Pro
XR_002956289.1:n.4898T>C
NM_001363725.2:c.2452T>C	NP_001350654.1:p.Ser818Pro
NM_001371656.1:c.4831T>C	NP_001358585.1:p.Ser1611Pro
NM_001374820.1:c.4831T>C	NP_001361749.1:p.Ser1611Pro
NM_001374828.1:c.4951T>C MANE Select	NP_001361757.1:p.Ser1651Pro
NM_017519.3:c.4792T>C	NP_059989.3:p.Ser1598Pro